Canonical Allele Identifier: CA410637910

Gene: PRODH DGCR6

Linked Data

• MyVariant Identifiers: chr22:g.18900781G>C (hg19) ; chr22:g.18913268G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913268G>C , CM000684.2:g.18913268G>C	GRCh38
NC_000022.10:g.18900781G>C , CM000684.1:g.18900781G>C	GRCh37
NC_000022.9:g.17280781G>C	NCBI36
NG_008226.2:g.28286C>G
NG_009052.1:g.12046G>C
NG_008226.3:g.28286C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1710C>G (PRODH) MANE Select	ENSP00000349577.6:p.Ser570Arg
ENST00000638240.1:c.513+2240G>C	ENSP00000492446.1:n.513+2240G>C
ENST00000313755.9:n.2475C>G (PRODH)
ENST00000334029.6:c.1386C>G (PRODH)	ENSP00000334726.2:p.Ser462Arg
ENST00000357068.10:c.1710C>G (PRODH)	ENSP00000349577.6:p.Ser570Arg
ENST00000420436.5:c.1386C>G (PRODH)	ENSP00000410805.1:p.Ser462Arg
ENST00000429300.5:n.2081C>G (PRODH)
ENST00000482858.5:n.4190C>G (PRODH)
ENST00000483718.5:c.*1910G>C (DGCR6)	ENSP00000467483.1:n.*1910G>C
ENST00000491604.5:n.2619C>G (PRODH)
ENST00000610940.4:c.1710C>G (PRODH)	ENSP00000480347.1:p.Ser570Arg
NM_001195226.1:c.1386C>G (PRODH)	NP_001182155.1:p.Ser462Arg
NM_016335.4:c.1710C>G (PRODH)	NP_057419.4:p.Ser570Arg
XM_011530278.1:c.1137C>G (PRODH)	XP_011528580.1:p.Ser379Arg
XM_011530279.1:c.930C>G (PRODH)	XP_011528581.1:p.Ser310Arg
XR_937876.1:n.1777C>G (PRODH)
NM_005675.5:c.*1579G>C (DGCR6)	NP_005666.2:n.*1579G>C
NM_001195226.2:c.1386C>G (PRODH)	NP_001182155.2:p.Ser462Arg
NM_016335.5:c.1710C>G (PRODH)	NP_057419.5:p.Ser570Arg
NM_016335.6:c.1710C>G (PRODH) MANE Select	NP_057419.5:p.Ser570Arg